Malley A, Dresser D W
Immunology. 1983 Jan;48(1):93-9.
A method is described for using mini-Marbrook chambers for culturing spleen cells together with anti-idiotype antibody (anti-Id) to induce the appearance of suppressor T cells (Ts). Spleen cells that have been cultured with affinity prepared anti-Id (IgG) but not those cultured with normal IgG, suppress a secondary IgE response to timothy grass pollen antigen B (AgB) when injected intravenously into AGB-primed and boosted syngeneic recipient mice. Suppressor T cells are not induced if the spleen cells cultured with anti-Id are depleted of B cells of if the cells are cultured with the F(ab)2 fragment of anti-Id: both of these results are compatible with Fc+ cells playing a role in the induction of Ts cells by anti-Id. Analysis of soluble suppressor factors in an ELISA test suggests that both TS1 and TS2 cells may be induced by anti-Id.
本文描述了一种使用微型马尔布鲁克培养室将脾细胞与抗独特型抗体(抗Id)一起培养以诱导抑制性T细胞(Ts)出现的方法。用亲和制备的抗Id(IgG)培养的脾细胞,而非用正常IgG培养的脾细胞,当静脉注射到经 Timothy 草花粉抗原B(AgB)致敏和加强免疫的同基因受体小鼠体内时,可抑制对该抗原的二次IgE反应。如果用抗Id培养的脾细胞中的B细胞被清除,或者细胞用抗Id的F(ab)2片段培养,则不会诱导出抑制性T细胞:这两个结果均表明Fc +细胞在抗Id诱导Ts细胞的过程中发挥作用。ELISA试验中对可溶性抑制因子的分析表明,TS1和TS2细胞都可能由抗Id诱导产生。